Hydrofuramide

Hydrofuramide
Names
	IUPAC name (E)-1-(Furan-2-yl)-N-[furan-2-yl-[(E)-furan-2-ylmethylideneamino]methyl]methanimine
	Other names N,N'-Difurfurylidene-2-furanmethanediamine
Identifiers
CAS Number	494-47-3 ;
3D model (JSmol)	Interactive image;
ChemSpider	7844541;
ECHA InfoCard	100.007.083
EC Number	207-790-8;
PubChem CID	9570073;
UNII	BI73W105SX ;
CompTox Dashboard (EPA)	DTXSID00871696 DTXSID30877702, DTXSID00871696 ;
	InChI InChI=1S/C15H12N2O3/c1-4-12(18-7-1)10-16-15(14-6-3-9-20-14)17-11-13-5-2-8-19-13/h1-11,15H/b16-10+,17-11+ Key: CYGDSXFTXXFMNI-OTYYAQKOSA-N; InChI=1/C15H12N2O3/c1-4-12(18-7-1)10-16-15(14-6-3-9-20-14)17-11-13-5-2-8-19-13/h1-11,15H/b16-10+,17-11+ Key: CYGDSXFTXXFMNI-OTYYAQKOBP;
	SMILES C1=COC(=C1)/C=N/C(/N=C/C2=CC=CO2)C3=CC=CO3;
Properties
Chemical formula	C15H12N2O3
Molar mass	268.272 g·mol−1
Appearance	crystals
Density	1.23 g/mL @ 20 °C
Melting point	118 to 119 °C (244 to 246 °F; 391 to 392 K)
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Hydrofuramide is a condensation product of three molar equivalents of furfural with two molar equivalents of ammonia. Hydrofuramide is a crystalline solid with a melting point of 118-119 °C.^[1] The molecule may be described as a diimine with three pendant furanyl rings. Hydrofuramide is a versatile specialty chemical with applications in diverse areas, including rubber additives, pharmaceutical intermediates, preservatives, and rodenticides.^[2]

^ Chin-Hsing Chou; Chu, Li-Tse; Chiu, Shao-Jung; Lee, Chin-Fan; She, Yao-Teng (2004). "Synthesis of N,N-di(arylmethylidene)arylmethanediamines by flash vacuum pyrolysis of arylmethylazides". Tetrahedron. 60 (31): 6581–6584. doi:10.1016/j.tet.2004.06.082.
^ G. Marches (1958). "Biological study of a new raticide substance, hydrofuramide". Acad. Rep. Populare Romine, Studii Cercetari Biol., Ser. "Biol. Animala". 10: 335–44.

[1] Chin-Hsing Chou; Chu, Li-Tse; Chiu, Shao-Jung; Lee, Chin-Fan; She, Yao-Teng (2004). "Synthesis of N,N-di(arylmethylidene)arylmethanediamines by flash vacuum pyrolysis of arylmethylazides". Tetrahedron. 60 (31): 6581–6584. doi:10.1016/j.tet.2004.06.082.

[Marches1958-2] G. Marches (1958). "Biological study of a new raticide substance, hydrofuramide". Acad. Rep. Populare Romine, Studii Cercetari Biol., Ser. "Biol. Animala". 10: 335–44.

[1]

[2]